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Title:  Manager - Analytical Development

Date:  Jul 4, 2025
Location:  Tandalja - R&D
Company:  Sun Pharmaceutical Industries Ltd
  • To work as per cGMP and ensure its compliance as per current guideline and SOPs.
  • Responsible to align with organization goal and other responsibilities assigned by reporting authority.
  • Responsible to perform the calibration of instrument and to maintain instrument/equipment as per SOPs.
  • Responsible to follow safety precaution as per laboratory procedure.
  • Responsible for method development studies of Drug Substance, Drug Product & In process Materials related to Peptides. 
  • Responsible for method Validation studies of Drug Substance, Drug Product & In process Materials related to Peptides. 
  • Responsible for analysis of routine samples and stability studies of Drug Product & In process Material Drug Substance, Drug Product & In process Materials related to Peptides. 
  • Responsible to prepare Study Protocol and Study Reports.
  • Responsible for analysis of Oligonucleotides (DNA & RNA molecules) of single strand (Sense and Antisense) and Duplexes molecules.
  • Responsible for Development of IEX and Ion Pair method for Sense and Antisense to separate charge variants in DNA and RNA molecules
  • Responsible for Development of SEC method to separate size variants in DNA and RNA molecules.
  • Responsible for Isolation of Peptide molecules from impurities by PREP HPLC.

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